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TCTTGGGCATCTTCTTGGAGACTTT[A/G]AAGAAACTCGTGTCCCCTTTGTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616251 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TCAF1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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TCAF1 - TRPM8 channel associated factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206938.1 | 918 | Silent Mutation | NP_001193867.1 | |||
NM_001206941.1 | 918 | Intron | NP_001193870.1 | |||
NM_014719.2 | 918 | Silent Mutation | NP_055534.1 | |||
XM_005250074.3 | 918 | Missense Mutation | XP_005250131.1 | |||
XM_005250075.2 | 918 | Missense Mutation | XP_005250132.1 | |||
XM_005250076.3 | 918 | Intron | XP_005250133.1 | |||
XM_005250077.2 | 918 | Missense Mutation | XP_005250134.1 | |||
XM_006716191.2 | 918 | Missense Mutation | XP_006716254.1 | |||
XM_006716192.3 | 918 | Missense Mutation | XP_006716255.1 | |||
XM_017012833.1 | 918 | Missense Mutation | XP_016868322.1 | |||
XM_017012834.1 | 918 | Missense Mutation | XP_016868323.1 | |||
XM_017012835.1 | 918 | Missense Mutation | XP_016868324.1 | |||
XM_017012836.1 | 918 | Missense Mutation | XP_016868325.1 |